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149 Products found on IFF Pharma Solutions

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Avicel® PH - 103 banner
IFF Pharma SolutionsAvicel® PH - 103
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Granules, Tablets, Suspension
  • Labeling Claims:Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Not Tested on Animals, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Genotoxic-free, Ethylene Glycol-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, PAH-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Kosher, Amine-free, Dioxane-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Potassium-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003, IFANCA Halal
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
Avicel® PH - 103 is a microcrystalline cellulose used in direct compression, dry granulation, and wet granulation technologies. It serves the healthcare and pharma markets, particularly in oral drug delivery and care solutions. This product is available in granule form.
Avicel® CE-15 banner
IFF Pharma SolutionsAvicel® CE-15
  • Chemical Name:Guar Gum, Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
  • Dosage Form:Soft Chews, Tablets
  • Labeling Claims:Not Tested on Animals, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, TSE-free, Vegetarian, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, Kosher, Perchlorate-free, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Not Engineered With Nanomaterials, Preservative-free, PFAS-Free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, EC No. 1935/2004, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, EU Directive 2002/72/EC, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 10/2011 (PIM), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, FCC Compliant, British Pharmacopeia (BP), ISO 45001, Directive 1895/2005/EC, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, EC No. 2023/2006, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, IFANCA Halal, IFRA Compliant
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
Avicel® CE-15 a non-animal-derived ingredient, is widely employed in tablet production. It's adaptable to various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceutical and nutraceutical applications, it acts as a binder, compression aid, filler, immediate release agent, and suspension aid. It's supplied in powder form for easy tablet formulation.
Protanal® CR - 8133 banner
IFF Pharma SolutionsProtanal® CR - 8133
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Protanal® CR - 8133 featuring sodium alginate, serves various functions in pharmaceuticals and nutraceuticals. It acts as an antacid, controlled release agent, emulsifying agent, gelling agent, thickener, and viscosity modifier, available in powder form.
Protanal® KF200 RBS banner
IFF Pharma SolutionsProtanal® KF200 RBS
  • Chemical Name:Potassium Alginate
  • CAS Number:9005-36-1
  • Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Protanal® KF200 RBS available in powder form, serves multiple functions in pharmaceuticals and nutraceuticals. It acts as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, offering versatile applications in various formulations.
Protanal® AR - 1410 banner
IFF Pharma SolutionsProtanal® AR - 1410
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Steroids Free, No Artificial Sweeteners, Colorants-free, Copper-free, Natural Latex Rubber-Free, Naturally Derived, Halal, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, NPE-free, Pareve, Herbicide-free, Solvent-free, Perfluorocarbon (PFC)-free, Mycotoxins-free, Residual Solvent -Free, APE-free, Caffeine Free, Plant-Based, Barium-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Cobalt-free, Gold-Free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Cadmium-free, Palm Oil-free, Bactericide-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Radioactive-free, GMO-free, Kosher, Tin-free, Preservative-free, PFAS-Free, Conflict minerals-free, Nanomaterials-free, Potassium-free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FFDCA, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Protanal® AR - 1410 is a versatile powder designed for various functions in the pharmaceutical and nutraceutical industries. It serves as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid, ensuring optimal performance in formulations. Crafted to be sewage sludge-free, it meets high standards of quality and safety.
METHOCEL™ K4M Premium HPMC banner
IFF Pharma SolutionsMETHOCEL™ K4M Premium HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Controlled Release Agent, Suspending Agent, Binder, Thickener, Mucoadhesive, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Tablets
  • Labeling Claims:VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ K4M Premium HPMC utilized in ceramics and pharmaceuticals, serves as a binder, film former, gelling agent, mucoadhesive, solubilizer, and suspension aid. It aids in granulation and exhibits water solubility.
Protacid® AR - 1112 banner
IFF Pharma SolutionsProtacid® AR - 1112
  • Chemical Name:Alginic Acid
  • CAS Number:9005-32-7
  • Functions:Antacid, Controlled Release Agent
  • Labeling Claims:Dye Free, Plasticizer-free, Nanomaterials-free, APE-free, Triphenyl Tin Compounds-Free, Residual Solvent -Free, Halal, Paraben-free, Propylene Glycol-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Solvent-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Melamine-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), EC No. 2023/2006, Kosher, European Regulation 396/2005/EC, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, ISO 14001, Regulation (EU) No. 1272/2008, Halal Food Council of Europe, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ISO 9000, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS)
  • Chemical Inventories:PICCS (Phillipines)
Protacid® AR - 1112 primarily composed of alginic acid, offers various benefits, such as being free of APE, bisphenol A, caffeine, and colorants. In pharmaceutical and nutraceutical applications, it functions as an antacid and controlled release agent. Its physical form is a powder, ensuring ease of handling and formulation.
METHOCEL™ K200M Premium HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ K200M Premium HPMC - Specialty
  • Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener, Binder, Emulsifier
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Dosage Form:Tablets
  • Certifications & Compliance:Regulation (EC) No. 1333/2008, FDA 21 CFR 176.170, Waste Electrical & Electronic Equipment Directive (WEEE), cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Swiss Ordinance (SR 817.023.21), Organic Certified, Chinese Pharmacopeia (ChP), European Pharmacopeia (Ph. Eur.), USDA Organic, Kosher, FDA 21 CFR 182.1480, FFDCA, ICH Q3C, FSC Certified, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, Belgian Law And Codex Alimentarius Standards, FDA 21 CFR 175.105, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), FDA 21 CFR 175.300, FDA 21 CFR 176.180, British Pharmacopeia (BP), EXCiPACT, FDA 21 CFR 174.5, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Nagoya Compliant, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS)
  • Features:Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range
METHOCEL™ K200M Premium HPMC - Specialty identified as cellulose ethers and hypromellose, serves a wide array of functions across capsules, suspensions, tablets, granulation, and tablet coating applications. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, thickener, and viscosity modifier. Notably, it is water-soluble, ensuring versatility and efficacy in formulations.
Endurance® VE - 102 banner
IFF Pharma SolutionsEndurance® VE - 102
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Functions:Binder
  • Manufacturing Technology:Direct Compression, Wet Granulation
  • Labeling Claims:Dye Free, Plasticizer-free, APE-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Ethylene Oxide-free, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Solvent-free, Not Tested on Animals, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free, PFAS-Free, Zinc-free, Aluminum-free, Endocrine Disruptor-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Kosher, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), ISO 45001, ISO 14001, Orthodox Union Kosher, National Formulary (NF), FCC Compliant, ISO 22000, Generally Recognized As Safe (GRAS)
Endurance® VE - 102 comprising microcrystalline cellulose, finds applications in dietary supplements. It functions as a binder in food and nutrition, as well as in pharmaceuticals and nutraceuticals, presenting as a powder.
Ac-Di-Sol® SD - 711 banner
IFF Pharma SolutionsAc-Di-Sol® SD - 711
  • Chemical Name:Croscarmellose Sodium
  • CAS Number:74811-65-7
  • Dosage Form:Orally Disintegrating Tablets (ODTs), Granules, Capsules
  • Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, USP 232 Elemental Impurities Free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR Regulations, FCC Compliant, British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, FSSC 22000, Orthodox Union Kosher, Regulation (EU) No. 1169/2011, IFANCA Halal, China DMF
  • Manufacturing Technology:Wet Granulation
Ac-Di-Sol® SD - 711 a powdered form of croscarmellose sodium, is utilized as a disintegrant and immediate release agent in pharmaceuticals and nutraceuticals. Its versatility is evident in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs), manufactured through wet granulation techniques.

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